US20230142429A1 - Process for production of new sulfolenic intermediates - Google Patents
Process for production of new sulfolenic intermediates Download PDFInfo
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- US20230142429A1 US20230142429A1 US17/915,448 US202117915448A US2023142429A1 US 20230142429 A1 US20230142429 A1 US 20230142429A1 US 202117915448 A US202117915448 A US 202117915448A US 2023142429 A1 US2023142429 A1 US 2023142429A1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/46—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings substituted on the ring sulfur atom
- C07D333/48—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings substituted on the ring sulfur atom by oxygen atoms
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- the present invention relates to a new process for the production of new specific intermediates, which are preferably used in the production of vitamin A, vitamin A acetate, or ⁇ -carotene and derivatives thereof, e.g. canthaxanthin, astaxanthin or zeaxanthin.
- the new compounds are useful as intermediates (building blocks) in the synthesis of vitamin A or ⁇ -carotene, preferably vitamin A.
- Vitamin A plays a role in a variety of functions throughout the body, such as e.g. vision process, gene transcription, immune function, bone metabolism, haematopoiesis, skin and cellular health and antioxidant function.
- the goal of the present invention was to find easily accessible compounds, which can then be used in an improved synthesis of vitamin A or its derivates, or ⁇ -carotene, preferably vitamin A (acetate).
- the aim was achieved by the synthesis as disclosed and described below.
- R is H, or —(CO)—(CH 2 ) n CH 3 , wherein n has a value of 0-14, or
- R is —X(C 1-4 alkyl) 3 or —X(C 6 H 5 ) 3 , wherein X is Si or Ge
- R is tetrahydro pyrane, isopropylmethyl ether or 2-methoxy-butylether,
- R is H, or —(CO)—(CH 2 ) n CH 3 , wherein n has a value of 0-14, or
- R is —X(C 1-4 alkyl) 3 or —X(C 6 H 5 ) 3 , wherein X is Si or Ge
- R is tetrahydro pyrane, isopropylmethyl ether or 2-methoxy-butylether.
- the present invention relates to a process (P) for the production of a compound of formula (I)
- R is H, or —(CO)—(CH 2 ) n CH 3 , wherein n has a value of 0-14, preferably 0-10, more preferably 0 or 1, most preferably 1, or
- R is —X(C 1-4 alkyl) 3 or —X(C 6 H 5 ) 3 , wherein X is Si or Ge,
- R is tetrahydro pyrane, isopropylmethyl ether or 2-methoxy-butylether,
- R has the same meanings as defined for the compound of formula (I).
- the present invention also relates to a process (P′) for the production of a compound of formula (I)
- R is H, or —(CO)—(CH 2 ) n CH 3 , wherein n has a value of 0-10.
- the present invention also relates to a process (P′′) for the production of a compound of formula (I)
- R is H, or —(CO)—(CH 2 ) n CH 3 , wherein n has a value of 0 or 1.
- the present invention also relates to a process (P′′′) for the production of a compound of formula (I)
- R is H, or —(CO)—(CH 2 ) CH 3 .
- the present invention also relates to a process (P′′′′) for the production of a compound of formula (I)
- R is —X(C 1-4 alkyl) 3 or —X(C 6 H 5 ) 3 , wherein X is Si or Ge.
- the present invention also relates to a process (P′′′′′) for the production of a compound of formula (I)
- R is tetrahydro pyrane, isopropylmethyl ether or 2-methoxy-butylether.
- the process according to the present invention is usually carried out in the presence of a strong base such as Schlesinger base, 2,2,6,6-tetramethyl piperidine, lithium diisopropylamide, n-butyllithium, hexyllithium, tert.-butyl lithium, sec-butyllithium, metal amide (with metals such as Na, K and Cs), lithium hexamethyldisilazane, metal hydride (with metals such as Na, Mg, K and Cs), metal hydroxide (with metals such as Na, K and Cs), metal alkoxide (with metals such Na, K and Cs) or sodium hexamethyl-disilazane.
- a strong base such as Schlesinger base, 2,2,6,6-tetramethyl piperidine, lithium diisopropylamide, n-butyllithium, hexyllithium, tert.-butyl lithium, sec-butyllithium, metal amide
- the present invention relates to the process (P1), which is process (P), (P′), (P′′), (P′′′), (P′′′′) or (P′′′′′), wherein the process is carried out in the presence of at least one strong base.
- the present invention relates to the process (P1′), which is process (P1), wherein the at least one strong base is chosen from the group consisting of Schlesinger base, 2,2,6,6-tetramethyl piperidine, lithium diisopropylamide, n-butyllithium, hexyllithium, tert.-butyl lithium, sec-butyllithium, metal amide (wherein the metals are chosen from the group consisting of Na, K and Cs), lithium hexamethyldisilazane, metal hydride (wherein the metals are chosen from the group consisting of Na, Mg, K and Cs), metal hydroxide (wherein the metals are chosen from the group consisting of Na, K and Cs), metal alkoxide (wherein the metals are chosen from the group consisting of Na, K and Cs) and sodium hexamethyl-disilazane.
- the at least one strong base is chosen from the group consisting of Schlesinger base, 2,2,6,6
- the process is usually carried out in an inert solvent.
- the solvent is a polar aprotic solvent. More preferably the solvent is chosen from the group consisting of pyridine, toluene, xylene, THF, methyl THF, or ethers (such as diethylether, 1,4-dioxane, 1,2-dimethoxyethane and crown ethers).
- one solvent can also be a nonpolar solvent (such as heptane, n-pentane, and other hydrocarbones).
- the present invention relates to the process (P2), which is process (P), (P′), (P′′), (P′′′), (P′′′′), (P′′′′′), (P1) or (P1′), wherein the process is carried out in at least one inert solvent.
- the present invention relates to the process (P2′), which is process (P2), wherein the solvent is a polar aprotic solvent.
- the present invention relates to the process (P2′′), which is process (P2) or (P4′), wherein the at least one solvent is chosen from the group consisting of pyridine, toluene, xylene, THF, methyl THF, and ethers.
- the present invention relates to the process (P2′′′), which is process (P2) or (P4′), wherein the at least one solvent is chosen from the group consisting of pyridine, toluene, xylene, THF, methyl THF, and ethers chosen from the group consisting of diethylether, 1,4-dioxane, 1,2-dimethoxyethane and crown ethers.
- the at least one solvent is chosen from the group consisting of pyridine, toluene, xylene, THF, methyl THF, and ethers chosen from the group consisting of diethylether, 1,4-dioxane, 1,2-dimethoxyethane and crown ethers.
- the process according to the present invention is usually carried out at low temperature. Usually a temperature range of from ⁇ 100° C. to 25° C., preferably at a temperature range of from ⁇ 95° C. to 5° C.
- the present invention relates to the process (P3), which is process (P), (P′), (P′′), (P′′′), (P′′′′), (P′′′′′), (P1), (P1′), (P2), (P2′), (P2′′) or (P2′′′), wherein the process is carried out at a temperature range of from ⁇ 100° C. to 25° C.
- the present invention relates to the process (P3′), which is process (P), (P′), (P′′), (P′′′), (P′′′′), (P′′′′′), (P1), (P1′), (P2), (P2′), (P2′′) or (P2′′′), wherein the process is carried out at a temperature range of from ⁇ 95° C. to 5° C.
- the starting material which are the compounds of formula (II) and of formula (III) can be used in equimolar amounts. But it is also possible to use an excess of one of the starting material. Usually the molar ratio of the compound of formula (II) to the compound of formula (III) goes from 1:2 to 2:1.
- the present invention relates to the process (P4), which is process (P), (P), (P′), (P′′), (P′′′), (P′′′′), (P′′′′′), (P1), (P1′), (P2), (P2′), (P2′′), (P2′′′), (P3) or (P3′), wherein the molar ratio of the compound of formula (II) to the compound of formula (III) goes from 1:2 to 2:1.
- R is H, or —(CO)—(CH 2 ) n CH 3 , wherein n has a value of 0-14, or
- R is —X(C 1-4 alkyl) 3 or —X(C 6 H 5 ) 3 , wherein X is Si or Ge,
- R is tetrahydro pyrane, isopropylmethyl ether or 2-methoxy-butylether.
- the present invention relates to compounds of formula (I)
- R is —(CO)—(CH 2 ) n CH 3 , wherein n has a value of 0-10.
- the present invention relates to compounds of formula (I)
- R is —(CO)—(CH 2 ) n CH 3 , wherein n has a value of 0 or 1.
- the present invention relates to the compound of formula (I)
- R is —(CO)—(CH 2 )CH 3 .
- the following schema shows how to produce vitamin A (or derivatives thereof) can be obtained.
- R has the same meanings are defined above.
- the temperature is given in ° C. and all percentages are related to the weight.
- the crude was purified with a column chromatography (SiO2) to obtain the products in 45% yield.
- the reaction mixture was stirred at ⁇ 76° C. for 7 min. Subsequently the cooling bath was removed and half saturated ammonium chloride solution (5 mL) was added.
- the reaction mixture was diluted and extracted with toluene (10 mL).
- the aqueous layer was separated and extracted with toluene (10 mL).
- the organic layers were washed with water (2 ⁇ 10 mL) and saturated sodium chloride solution (1 ⁇ 10 mL).
- the combined organic layers were filtered over a plug of cotton wool. All volatiles were evaporated at 40° C. (5 mbar) until a clear yellow oil remained.
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Abstract
The present invention relates to a new process for the production of new specific intermediates, which are preferably used in the production of vitamin A, vitamin A acetate, or β-carotene and derivatives thereof, e.g. canthaxanthin, astaxanthin or zeaxanthin.
Description
- The present invention relates to a new process for the production of new specific intermediates, which are preferably used in the production of vitamin A, vitamin A acetate, or β-carotene and derivatives thereof, e.g. canthaxanthin, astaxanthin or zeaxanthin. Especially to be mentioned is that the new compounds are useful as intermediates (building blocks) in the synthesis of vitamin A or β-carotene, preferably vitamin A.
- Vitamin A or its derivatives such as Vitamin acetate
- is an important ingredient for many applications. Vitamin A plays a role in a variety of functions throughout the body, such as e.g. vision process, gene transcription, immune function, bone metabolism, haematopoiesis, skin and cellular health and antioxidant function.
- Due to the importance of vitamin A (and its derivatives) and the complexity of the synthesis thereof, there is always a need for improved processes of production.
- The goal of the present invention was to find easily accessible compounds, which can then be used in an improved synthesis of vitamin A or its derivates, or β-carotene, preferably vitamin A (acetate). The aim was achieved by the synthesis as disclosed and described below.
- The new intermediates, which are produced by the process according to the present invention are the compounds of formula (I)
- wherein
- R is H, or —(CO)—(CH2)nCH3, wherein n has a value of 0-14, or
- R is —X(C1-4alkyl)3 or —X(C6H5)3, wherein X is Si or Ge
- or R is tetrahydro pyrane, isopropylmethyl ether or 2-methoxy-butylether,
- which are ideal intermediates (especially) in the vitamin A (and/or its derivates) production.
- How vitamin A (and/or its derivatives) are obtained is disclosed and discussed further below.
- The compounds of formula (I), (II) and (III) have several diastereoisomeric forms. Also when not explicitly disclosed all of these forms are all claimed and disclosed by the Markush formulae of these compounds in the present patent application.
- To obtain a compound of formula (I), the compound of formula (II)
- is reacted with a compound of formula (III)
- wherein
- wherein R is H, or —(CO)—(CH2)nCH3, wherein n has a value of 0-14, or
- R is —X(C1-4alkyl)3 or —X(C6H5)3, wherein X is Si or Ge
- or R is tetrahydro pyrane, isopropylmethyl ether or 2-methoxy-butylether.
- Therefore the present invention relates to a process (P) for the production of a compound of formula (I)
- wherein
- R is H, or —(CO)—(CH2)nCH3, wherein n has a value of 0-14, preferably 0-10, more preferably 0 or 1, most preferably 1, or
- R is —X(C1-4alkyl)3 or —X(C6H5)3, wherein X is Si or Ge,
- or
- R is tetrahydro pyrane, isopropylmethyl ether or 2-methoxy-butylether,
- characterized in that the compound of formula (II)
- is reacted with a compound of formula (III)
- wherein R has the same meanings as defined for the compound of formula (I).
- Therefore the present invention also relates to a process (P′) for the production of a compound of formula (I)
- wherein
- R is H, or —(CO)—(CH2)nCH3, wherein n has a value of 0-10.
- Therefore the present invention also relates to a process (P″) for the production of a compound of formula (I)
- wherein
- R is H, or —(CO)—(CH2)nCH3, wherein n has a value of 0 or 1.
- Therefore the present invention also relates to a process (P′″) for the production of a compound of formula (I)
- wherein
- R is H, or —(CO)—(CH2) CH3.
- Therefore the present invention also relates to a process (P″″) for the production of a compound of formula (I)
- wherein
- R is —X(C1-4alkyl)3 or —X(C6H5)3, wherein X is Si or Ge.
- Therefore the present invention also relates to a process (P′″″) for the production of a compound of formula (I)
- wherein
- R is tetrahydro pyrane, isopropylmethyl ether or 2-methoxy-butylether.
- It is known from the prior art how to obtain the compounds of formula (II) (e.g. from Desai et al. Tetrahedron, 1992, 48, 481-490 or from Kienzle et al. Helvetica Chimica Acta, 1975, 58, 27-40.)
- The process according to the present invention is usually carried out in the presence of a strong base such as Schlesinger base, 2,2,6,6-tetramethyl piperidine, lithium diisopropylamide, n-butyllithium, hexyllithium, tert.-butyl lithium, sec-butyllithium, metal amide (with metals such as Na, K and Cs), lithium hexamethyldisilazane, metal hydride (with metals such as Na, Mg, K and Cs), metal hydroxide (with metals such as Na, K and Cs), metal alkoxide (with metals such Na, K and Cs) or sodium hexamethyl-disilazane.
- Therefore the present invention relates to the process (P1), which is process (P), (P′), (P″), (P′″), (P″″) or (P′″″), wherein the process is carried out in the presence of at least one strong base.
- Therefore the present invention relates to the process (P1′), which is process (P1), wherein the at least one strong base is chosen from the group consisting of Schlesinger base, 2,2,6,6-tetramethyl piperidine, lithium diisopropylamide, n-butyllithium, hexyllithium, tert.-butyl lithium, sec-butyllithium, metal amide (wherein the metals are chosen from the group consisting of Na, K and Cs), lithium hexamethyldisilazane, metal hydride (wherein the metals are chosen from the group consisting of Na, Mg, K and Cs), metal hydroxide (wherein the metals are chosen from the group consisting of Na, K and Cs), metal alkoxide (wherein the metals are chosen from the group consisting of Na, K and Cs) and sodium hexamethyl-disilazane.
- The process is usually carried out in an inert solvent. Preferably the solvent is a polar aprotic solvent. More preferably the solvent is chosen from the group consisting of pyridine, toluene, xylene, THF, methyl THF, or ethers (such as diethylether, 1,4-dioxane, 1,2-dimethoxyethane and crown ethers).
- It is also possible to have a mixture of solvents, wherein one solvent can also be a nonpolar solvent (such as heptane, n-pentane, and other hydrocarbones).
- Therefore the present invention relates to the process (P2), which is process (P), (P′), (P″), (P′″), (P″″), (P′″″), (P1) or (P1′), wherein the process is carried out in at least one inert solvent.
- Therefore the present invention relates to the process (P2′), which is process (P2), wherein the solvent is a polar aprotic solvent.
- Therefore the present invention relates to the process (P2″), which is process (P2) or (P4′), wherein the at least one solvent is chosen from the group consisting of pyridine, toluene, xylene, THF, methyl THF, and ethers.
- Therefore the present invention relates to the process (P2′″), which is process (P2) or (P4′), wherein the at least one solvent is chosen from the group consisting of pyridine, toluene, xylene, THF, methyl THF, and ethers chosen from the group consisting of diethylether, 1,4-dioxane, 1,2-dimethoxyethane and crown ethers.
- The process according to the present invention is usually carried out at low temperature. Usually a temperature range of from −100° C. to 25° C., preferably at a temperature range of from −95° C. to 5° C.
- Therefore the present invention relates to the process (P3), which is process (P), (P′), (P″), (P′″), (P″″), (P′″″), (P1), (P1′), (P2), (P2′), (P2″) or (P2′″), wherein the process is carried out at a temperature range of from −100° C. to 25° C.
- Therefore the present invention relates to the process (P3′), which is process (P), (P′), (P″), (P′″), (P″″), (P′″″), (P1), (P1′), (P2), (P2′), (P2″) or (P2′″), wherein the process is carried out at a temperature range of from −95° C. to 5° C.
- The starting material, which are the compounds of formula (II) and of formula (III) can be used in equimolar amounts. But it is also possible to use an excess of one of the starting material. Usually the molar ratio of the compound of formula (II) to the compound of formula (III) goes from 1:2 to 2:1.
- Therefore the present invention relates to the process (P4), which is process (P), (P), (P′), (P″), (P′″), (P″″), (P′″″), (P1), (P1′), (P2), (P2′), (P2″), (P2′″), (P3) or (P3′), wherein the molar ratio of the compound of formula (II) to the compound of formula (III) goes from 1:2 to 2:1.
- The obtained products of the process according to the present invention (these are the compound of formula (I)) are new ideal intermediates. Especially in the production of vitamin A and its derivates.
- Therefore the present invention relates to compounds of formula (I)
- wherein
- R is H, or —(CO)—(CH2)nCH3, wherein n has a value of 0-14, or
- R is —X(C1-4alkyl)3 or —X(C6H5)3, wherein X is Si or Ge,
- or
- R is tetrahydro pyrane, isopropylmethyl ether or 2-methoxy-butylether.
- Preferably, the present invention relates to compounds of formula (I)
- wherein R is —(CO)—(CH2)nCH3, wherein n has a value of 0-10.
- More preferably, the present invention relates to compounds of formula (I)
- wherein R is —(CO)—(CH2)nCH3, wherein n has a value of 0 or 1.
- Most preferably, the present invention relates to the compound of formula (I)
- wherein R is —(CO)—(CH2)CH3.
- The following schema shows how to produce vitamin A (or derivatives thereof) can be obtained.
- R has the same meanings are defined above.
- The following example serve to illustrate the invention. The temperature is given in ° C. and all percentages are related to the weight.
- 3-Methyl-2-((2,6,6-trimethylcyclohex-1-en-1-yl)methyl)-2,5-dihydrothiophene 1,1-dioxide (5.65 g, 20.1 mmol; 1.0 eq), (E)-3-methyl-4-oxobut-2-en-1-yl acetate (2.95 g, 20.8 mmol; 1.03 eq) and dry tetrahydrofuran (40.0 mL) were placed in a dried four necked round bottom flask equipped with a magnetic stirrer, thermometer and condenser under an argon atmosphere. The reaction mixture was cooled to −76° C. Lithium diisopropylamide (20.0 mL, 20.0 mmol, 0.99 eq, 1 M in tetrahydrofuran/hexane, d=0.719 g/mL) was added dropwise over a period of 40 min. The reaction was stirred at −76° C. for 2 h. Subsequently, the cooling bath was removed and half saturated ammonium chloride solution (100 mL) was added. The reaction mixture was diluted with diethylether (150 mL). The aqueous layer was separated and extracted with diethylether (150 mL). The organic layers were washed with half saturated ammonium chloride solution (100 mL), water (2×100 mL) and saturated sodium chloride solution (100 mL). The combined organic layers were filtered over a plug of cotton wool. All volatiles were evaporated at 40° C. (5 mbar).
- The crude was purified with a column chromatography (SiO2) to obtain the products in 45% yield.
- (E)-4-hydroxy-3-methyl-4-(4-methyl-1,1-dioxido-5-((2,6,6-trimethylcyclohex-1-en-1-yl)methyl)-2,5-dihydrothiophen-2-yl)but-2-en-1-yl acetate (55 mg, 0.13 mmol; 1.0 eq) and pyridine (3.0 mL) were placed in a dried two necked round bottom flask equipped with a magnetic stirrer and condenser under an argon atmosphere. The reaction mixture was heated to 100° C. for 5 h. All volatiles were evaporated under reduced pressure (50° C., 5 mbar) to obtain the product in 82% yield
- (E)-4-hydroxy-3-methyl-4-(4-methyl-1,1-dioxido-5-((2,6,6-trimethylcyclohex-1-en-1-yl)methyl)-2,5-dihydrothiophen-2-yl)but-2-en-1-yl acetate (product obtained from Example 1) (263 mg, 0.6 mmol; 1.0 eq) and dry toluene (5.0 mL) were placed in a dried two necked round bottom flask equipped with a magnetic stirrer and condenser under an argon atmosphere. The reaction mixture was heated to reflux for 2 h. All volatiles were evaporated under reduced pressure (40° C., 5 mbar) to obtain the product in a yield of 71%.
- 3-Methyl-2-((2,6,6-trimethylcyclohex-1-en-1-yl)methyl)-2,5-dihydrothiophene 1,1-dioxide (310 mg, 1.1 mmol; 1.0 eq), (E)-3-methyl-4-oxobut-2-en-1-yl propionate (190 mg, 1.2 mmol; 1.1 eq) and dry toluene (2.0 mL) were placed in a dried two necked round bottom flask under an argon atmosphere. The reaction mixture was cooled to −76° C. Lithium diidopropylamide (1.2 mL, 1.2 mmol, 1.1 eq, 1 M in tetrahydrofuran/hexane, d=0.719 g/mL) was added over a period of 7 min. The reaction mixture was stirred at −76° C. for 7 min. Subsequently the cooling bath was removed and half saturated ammonium chloride solution (5 mL) was added. The reaction mixture was diluted and extracted with toluene (10 mL). The aqueous layer was separated and extracted with toluene (10 mL). The organic layers were washed with water (2×10 mL) and saturated sodium chloride solution (1×10 mL). The combined organic layers were filtered over a plug of cotton wool. All volatiles were evaporated at 40° C. (5 mbar) until a clear yellow oil remained.
- The oil was placed in a dried two necked round bottom flask and dissolved in toluene (5 mL) with a magnetic stirrer, condenser under an argon atmosphere. The reaction mixture was heated to reflux for 2 h. All volatiles were evaporated under reduced pressure (50° C., 5 mbar) to obtain the product (399 mg), yield=52%.
- 3-Methyl-2-((2,6,6-trimethylcyclohex-1-en-1-yl)methyl)-2,5-dihydrothiophene 1,1-dioxide (308 mg, 1.1 mmol; 1.0 eq), (E)-3-methyl-4-oxobut-2-en-1-yl acetate (161 mg, 1.1 mmol; 1.0 eq) and dry toluene (2.0 mL) were placed in a dried two necked round bottom flask equipped with a magnetic stirrer under an argon atmosphere. The reaction mixture was cooled to −76° C. Lithium diidopropylamide (1.2 mL, 1.2 mmol, 1.1 eq, 1 M in tetrahydrofuran/hexane, d=0.719 g/mL) was added dropwise over a period of 8 min. The reaction was stirred at −76° C. for 7 min. Subsequently, the cooling bath was removed and half saturated ammonium chloride solution (5 mL) was added. The reaction mixture was diluted with toluene (10 mL). The aqueous layer was separated and extracted with toluene (10 mL). The organic layers were washed with water (2×10 mL) and saturated sodium chloride solution (1×10 mL). The combined organic layers were filtered over a plug of cotton wool. All volatiles were evaporated at 40° C. (5 mbar).
- The oil was placed in a dried two necked round bottom flask and dissolved in toluene (5 mL) with a magnetic stirrer under an argon atmosphere. The reaction mixture was heated to reflux for 1 h. All volatiles were evaporated under reduced pressure (40° C., 5 mbar). Purification afforded the product in 34% yield.
Claims (12)
1. Process of the production of compounds of formula (I)
wherein
R is H, or —(CO)—(CH2)nCH3, wherein n has a value of 0-14 or
R is —X(C1-4alkyl)3 or —X(C6H5)3, wherein X is Si or Ge
or R is tetrahydro pyrane, isopropylmethyl ether or 2-methoxy-butylether,
wherein the compound of formula (II)
is reacted with the compound of formula (III)
wherein R has the same meanings as defined for the compound of formula (I).
2. Process according to claim 1 , wherein R is
R is H, or —(CO)—(CH2)nCH3, wherein n has a value of 0 or 1, or
R is —X(C1-4alkyl)3 or —X(C6H5)3, wherein X is Si or Ge
or R is tetrahydro pyrane, isopropylmethyl ether or 2-methoxy-butylether.
3. Process according to claim 1 , wherein the process is carried out in the presence of at least one strong base.
4. Process according to claim 3 , wherein the at least one strong base is chosen from the group consisting of Schlesinger base, 2,2,6,6-tetramethyl piperidine, lithium diisopropylamide, n-butyllithium, hexyllithium, tert.-butyl lithium, sec-butyllithium, metal amide, lithium hexamethyldisilazane, metal hydride, metal hydroxide, metal alkoxide and sodium hexamethyl-disilazane.
5. Process according to claim 1 , wherein the process is carried out in at least one inert solvent.
6. Process according to claim 5 , wherein the solvent is a polar aprotic solvent.
7. Process according to claim 5 , wherein the at least one solvent is chosen from the group consisting of pyridine, toluene, xylene, THF, methyl THF, and ethers (such as diethylether, 1,4-dioxane, 1,2-dimethoxyethane and crown ethers.
8. Process according to claim 1 , wherein the process is carried out at a temperature range of from −100° C. to 25° C.
9. Process according to claim 1 , wherein the molar ratio of the compound of formula (II) to the compound of formula (III) goes from 1:2 to 2:1.
11. Compounds according to claim 10 , wherein R is —(CO)—(CH2)nCH3 and n has a value of 0-10.
12. Compounds according to claim 10 , wherein R is —(CO)—(CH2)nCH3 and n has a value of 0 or 1.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP20167023 | 2020-03-31 | ||
EP20167023.9 | 2020-03-31 | ||
PCT/EP2021/057242 WO2021197889A1 (en) | 2020-03-31 | 2021-03-22 | Process for production of new sulfolenic intermediates |
Publications (1)
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